The Building of a Multicomponent Adsorption System and Its

碩士 === 元智工學院 === 化學工程學系 === 85 === In this study, a built-in-lab was modified flow-type adsorption system for multicomponent adsorption experiment such that the adsorption behaviors near industrial reaction conditions...

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Bibliographic Details
Main Authors: Lee, Kun-Shyan, 李昆諴
Other Authors: Sheng-Diann Lin
Format: Others
Language:zh-TW
Online Access:http://ndltd.ncl.edu.tw/handle/33474425155398152034
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Summary:碩士 === 元智工學院 === 化學工程學系 === 85 === In this study, a built-in-lab was modified flow-type adsorption system for multicomponent adsorption experiment such that the adsorption behaviors near industrial reaction conditions could be examined. Similar results obtained by the TCD and the Mass spectrometry detection for one-component adsorption experiments confirm the capability of the system. and the accuracy of uptake measured with this system was found better than 0.04 mmole. Besides, both the step and the integral experimental procedures showed very similar results, with the latter capable of resolving irreversible and reversible uptakes. Hydrogen and Cyclohexane would not adsorption on TiO2, as observed in one- component adsorption experiment, Benzene and Toluene both reversibly adsorption on TiO2 with the latter showing higher uptake at similar partial pressure condition. The pressure of Cyclohexane showed no effect on the Benzene adsorption isotherm on TiO2; However, the pressure of 500 torr H2 reduced Benzene uptake @ lower Benzene partial pressure but not at higher partial pressure; thus, the Benzene isothermwas changed from type IV to Type V. In the competitive adsorption between Benzene and Toluene over TiO2 the Benzene adsorption isotherm was not changed significantly but the Toluene isotherm was shifted to lower uptake values. Although the estimated adsorption constant for both Benzene and Toluene were lower that measured in the one-component experiment. The relative ratio of their adsorption constant was not changed. Benzene and Toluene adsorption over Pt powders were mostly irreversible; the Toluene showed higher uptake than Benzene under similar partial pressure condition. However, the estimated monolayer coverages showed that the average cross sectional area were much smaller than the van der Waal cross sectional area of the ring; therefor, the adsorption of Benzene or Toluene on Pt powder may not be flat lying. Besides, dehydrogenation occurred concurrently which Benzene and Toluene adsorption on Pt powder; the estimated evolved Hydrogen show nearly 0.004 molar ratio to the Benzene or Toluene uptake. In the competitive adsorption between Benzene and Toluene, the Toluene isotherm was not affected by the presence of Benzene but the Benzene isotherm was changed.